ChemicalBook--->CAS DataBase List--->5472-49-1

5472-49-1

5472-49-1 Structure

5472-49-1 Structure
IdentificationBack Directory
[Name]

N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE
[CAS]

5472-49-1
[Synonyms]

PIPERIDINOPROPYL CHLORIDE HCL
N-(3-CHLOROPROPYL)PIPERIDINE HCL
1-(3-CHLOROPROPYL)PIPERIDINE HCL 98%
piperidinopropylchloride,hydrochloride
1-(3-CHLOROPROPYL) PIPERIDINE HYDROCHLO&
3-Piperidinopropyl Chloride Hydrochloride
1-(3-chloropropyl)-piperidinhydrochloride
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE
1-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE
1-(3-chloropropyl)piperidine monohydrochloride
N-(3-Chloropropyl)piperidine hydrochloride,97%
1-(3-Chloropropyl)piperidine Hydrochloride >
1-(3-Chloropropyl)piperidine hydrochloride (1:1)
Piperidine,1-(3-chloropropyl)-,hydrochloride(1:1)
1-(3-Chloropropyl)piperidine monohydrochloride 97%
[EINECS(EC#)]

226-812-7
[Molecular Formula]

C8H17Cl2N
[MDL Number]

MFCD00012838
[MOL File]

5472-49-1.mol
[Molecular Weight]

198.13
Chemical PropertiesBack Directory
[Melting point ]

219-223 °C(lit.)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Water Solubility ]

Soluble in water
[form ]

Powder or Crystalline Powder
[color ]

White to yellow
[InChI]

InChI=1S/C8H16ClN.ClH/c9-5-4-8-10-6-2-1-3-7-10;/h1-8H2;1H
[InChIKey]

OBOBUDMMFXRNDO-UHFFFAOYSA-N
[SMILES]

N1(CCCCl)CCCCC1.Cl
[CAS DataBase Reference]

5472-49-1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[RTECS ]

TM6498600
[HS Code ]

29333990
Hazard InformationBack Directory
[Uses]

1-(3-Chloropropyl)piperidine Hydrochloride is used in preparation of Triazolotriazine derivatives as A2A receptor antagonists.
[Synthesis]

Piperidine

110-89-4

1-Bromo-3-chloropropane

109-70-6

N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE

5472-49-1

Hexahydropyridine (piperidine, 0.45 g, 5.3 mmol) and 1-bromo-3-chloropropane (5.2 g, 33 mmol) were dissolved in toluene (17.5 mL) and then tetra-n-ammonium hydrogensulfate (ammonium hydrogensulfate, 0.51 g, 1.5 mmol) and 25% aqueous sodium hydroxide solution (10 mL) were added. The reaction mixture was stirred at 40 °C for 3 hours. After completion of the reaction, the mixture was cooled to room temperature, the toluene layer was separated, washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After removal of sodium sulfate by filtration, hydrochloric acid/methanol solution (2 mL) was added to the filtrate and the mixture was subsequently concentrated. The resulting crude product was purified by recrystallization from methanol/ether to give N-(3-chloropropyl)piperidine hydrochloride (0.96 g, 91% yield) as white crystals.

[References]

[1] Patent: US6642228, 2003, B1. Location in patent: Page/Page column 76-77
Spectrum DetailBack Directory
[Spectrum Detail]

N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)MS
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)1HNMR
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)13CNMR
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)IR1
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)IR2
N-(3-CHLOROPROPYL)PIPERIDINE HYDROCHLORIDE(5472-49-1)Raman
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